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- Aymé S., Preus M. The Marshall and Stickler syndromes: objective rejection of lumping. J Med Genet. 1984 Feb;21(1):34–38. doi: 10.1136/jmg.21.1.34. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baraitser M. Marshall/Stickler syndrome. J Med Genet. 1982 Apr;19(2):139–140. doi: 10.1136/jmg.19.2.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cohen M. M., Knobloch W. H., Gorlin R. J. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome). Birth Defects Orig Artic Ser. 1971 Jun;7(7):83–86. [PubMed] [Google Scholar]
- Hall J. Stickler syndrome. Presenting as a syndrome of cleft palate, myopia and blindness inherited as a dominant trait. Birth Defects Orig Artic Ser. 1974;10(8):157–171. [PubMed] [Google Scholar]
- Insley J., Astley R. A bone dysplasia with deafness. Br J Radiol. 1974 May;47(557):244–251. doi: 10.1259/0007-1285-47-557-244. [DOI] [PubMed] [Google Scholar]
- KNIEST W. Zur Abgrenzung der Dysostosis enchondralis von der Chondrodystrophie. Z Kinderheilkd. 1952;70(6):633–640. [PubMed] [Google Scholar]
- Keith C. G., Dobbs R. H., Shaw D. G., Cottrall K. Abnormal facies, myopia, and short stature. Arch Dis Child. 1972 Oct;47(255):787–793. doi: 10.1136/adc.47.255.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kelly T. E., Wells H. H., Tuck K. B. The Weissenbacher-Zweymüller syndrome: possible neonatal expression of the Stickler syndrome. Am J Med Genet. 1982 Jan;11(1):113–119. doi: 10.1002/ajmg.1320110113. [DOI] [PubMed] [Google Scholar]
- Liberfarb R. M., Goldblatt A. Prevalence of mitral-valve prolapse in the Stickler syndrome. Am J Med Genet. 1986 Jul;24(3):387–392. doi: 10.1002/ajmg.1320240302. [DOI] [PubMed] [Google Scholar]
- Liberfarb R. M., Hirose T., Holmes L. B. The Wagner-Stickler syndrome-a genetic study. Birth Defects Orig Artic Ser. 1979;15(5B):145–154. [PubMed] [Google Scholar]
- MARSHALL D. Ectodermal dysplasia; report of kindred with ocular abnormalities and hearing defect. Am J Ophthalmol. 1958 Apr;45(4 Pt 2):143–156. [PubMed] [Google Scholar]
- Miny P., Lenz W. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome. Am J Med Genet. 1985 Jun;21(2):317–324. doi: 10.1002/ajmg.1320210214. [DOI] [PubMed] [Google Scholar]
- Nance W. E., Sweeney A. A recessively inherited chondrodystrophy. Birth Defects Orig Artic Ser. 1970 Oct;6(4):25–27. [PubMed] [Google Scholar]
- O'Donnell J. J., Sirkin S., Hall B. D. Generalized osseous abnormalities in the Marshall syndrome. Birth Defects Orig Artic Ser. 1976;12(5):299–314. [PubMed] [Google Scholar]
- Opitz J. M., France T., Herrmann J., Spranger J. W. The Stickler syndrome. N Engl J Med. 1972 Mar 9;286(10):546–547. doi: 10.1056/NEJM197203092861020. [DOI] [PubMed] [Google Scholar]
- STICKLER G. B., BELAU P. G., FARRELL F. J., JONES J. D., PUGH D. G., STEINBERG A. G., WARD L. E. HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc. 1965 Jun;40:433–455. [PubMed] [Google Scholar]
- WEISSENBACHER G., ZWEYMUELLER E. GLEICHZEITIGES VORKOMMEN EINES SYNDROMS VON PIERRE ROBIN UND EINER FETALEN CHONDRODYSPLASIE. Monatsschr Kinderheilkd. 1964 Jun;112:315–317. [PubMed] [Google Scholar]
- Winter R. M., Baraitser M., Laurence K. M., Donnai D., Hall C. M. The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity. Am J Med Genet. 1983 Oct;16(2):189–199. doi: 10.1002/ajmg.1320160209. [DOI] [PubMed] [Google Scholar]
- Zellweger H., Smith J. K., Grützner P. The Marshall syndrome: report of a new family. J Pediatr. 1974 Jun;84(6):868–871. doi: 10.1016/s0022-3476(74)80769-9. [DOI] [PubMed] [Google Scholar]
- van Balen A. T., Falger E. L. Hereditary hyaloideoretinal degeneration and palatoschisis. Arch Ophthalmol. 1970 Feb;83(2):152–162. doi: 10.1001/archopht.1970.00990030154006. [DOI] [PubMed] [Google Scholar]